Babytherm 8004/8010 open care units 에 대한 현장 안전성 서한
Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI)에 따르면, 해당 현장 안전성 서한 는
Slovenia
에서 Drägerwerk AG & Co. KGaA 에 의해 제조된 제품과 관련되어 있습니다.
이것은 무엇인가요?
현장 안전성 서한은 의료기기 제조사 또는 제조사 대리인이 시중에 유통되고 있는 자사 의료기기 제품에 대하여 취할 수 있는 조치를 알리는 소통방식입니다. 주요 대상층은 보건의료업계 종사자와 의료기기 사용자들입니다. 여기에는 회수(recall) 조치와 경고도 포함될 수 있습니다.
Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Slovenia.
데이터 추가 비고
원인
As part of our market and product monitoring we have become aware of a case in which
a babytherm 8004 without patient was operated in skin temperature mode with skin
temperature sensor to prepare it for use. ln skin temperature mode, the radiant warmer
output is controlled automatically until the set skin temperature is reached. as a result of
operating the temperature sensor without patient contact, the radiant warmer was
operated continuously at a high output ievel. during this forced continuous operation
under high thermal ioad, the heating element aged faster. a part became detached from
the heating element and fell onto the mattress tray where a towel caught fire. .